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After the plasma membrane carrier-mediated GSH release from the cell, GSH becomes accessible to the active site of - glutamyl transpeptidase, which catalyzes the breakdown of the GSH - glutamyl bond forming two fractions: The -glutamyl fraction and the cysteinyl-glycine by transferring the -glutamyl fraction to an amino acid acceptor, forming -glutamyl-amino acid

Further studies are needed to confirm the actual benefit of this molecule on metabolic liver diseases and define the best route of administration and the most appropriate dosage, allowing its use in clinical practice

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M., Muntner, P., Bosworth, H

E.BarlowD.OlshanD.NaganoK.BaronR.et al (2015)

The component loadings for each variable showed that the variance in PC1 was largely driven by positive loading scores for TNF- ( r = 0.923) with a contribution of 51.74%